Zymomonas mobilis ZM1이 생산하는 균체외 Levansucrase의 정제 및 특성

Purification and Characterization of an Extracellular Levansucrase from Zymomonas mobilis ZM1(ATCC 10988).

  • 송기방 (생명공학연구소 미생물대사공학RU) ;
  • 서정우 (생명공학연구소 미생물대사공학RU) ;
  • 주현규 (선문대학교 식량자원학과) ;
  • 이상기 (생명공학연구소 미생물대사공학RU)
  • 발행 : 1998.08.01

초록

An extracellular levansucrase, which catalyzes the formation of levan from sucrose, from the culture broth of Zymomonas mobilis ZM1 was purified by conventional column purification methods. The final purification yield was 18.3 fold of the crude enzyme from Z. mobilis, with 16.5 % of the enzyme recovered in the preparation step. The molecular weight of the enzyme was estimated to be 91,000 by Superose 12 gel filtration, and 45,000 by SDS-PAGE, indicating that levansucrase is a dimer. The optimum pH for the enzyme activity was around pH 4.0 for sucrose hydrolysis, and was around pH 5.0 for levan formation. The enzyme was inhibited by some metal ions, such as Hg$\^$2+/ and Cu2$\^$2+/, and 50% of inhibition was observed with 5mM EDTA. The enzyme activity was enhanced by the presence of detergent Triton X-100, but inhibited by SDS completely The enzyme catalyzes the liberation of reducing sugars, oligosacccharides and the formation of fructose polymer(levan). The enzyme also catalyzes the transfructosylation reaction of fructose moiety from sucrose to various sugar acceptor molecules, including sugar alcohols.

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